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GB1031407A - Improvements in or relating to polyesters - Google Patents

Improvements in or relating to polyesters

Info

Publication number
GB1031407A
GB1031407A GB44423/64A GB4442364A GB1031407A GB 1031407 A GB1031407 A GB 1031407A GB 44423/64 A GB44423/64 A GB 44423/64A GB 4442364 A GB4442364 A GB 4442364A GB 1031407 A GB1031407 A GB 1031407A
Authority
GB
United Kingdom
Prior art keywords
acids
acid
polyester
product
bis
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB44423/64A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hoechst AG Werk Kalle Albert
Original Assignee
Chemische Werke Albert
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Chemische Werke Albert filed Critical Chemische Werke Albert
Publication of GB1031407A publication Critical patent/GB1031407A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/68Polyesters containing atoms other than carbon, hydrogen and oxygen
    • C08G63/692Polyesters containing atoms other than carbon, hydrogen and oxygen containing phosphorus
    • C08G63/6924Polyesters containing atoms other than carbon, hydrogen and oxygen containing phosphorus derived from polycarboxylic acids and polyhydroxy compounds
    • C08G63/6928Polycarboxylic acids and polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/67Unsaturated compounds having active hydrogen
    • C08G18/68Unsaturated polyesters
    • C08G18/683Unsaturated polyesters containing cyclic groups
    • C08G18/686Unsaturated polyesters containing cyclic groups containing cycloaliphatic groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/68Polyesters containing atoms other than carbon, hydrogen and oxygen
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/78Preparation processes
    • C08G63/82Preparation processes characterised by the catalyst used

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyesters Or Polycarbonates (AREA)
  • Macromonomer-Based Addition Polymer (AREA)

Abstract

A fire-retardant polyester resin is obtained by reacting dicyclopentadiene with the reaction product from (A) one or more dicarboxylic acids and/or ester-forming derivatives thereof, (B) one or more bromine-containing carboxylic acids, (C) one or more condensable phosphorus-containing compounds, and (D) one or more polyhydroxy compounds and/or ester-forming derivatives thereof, at least 20% of the total equivalents of acids and hydroxy compounds containing an olefinic bond, and the bromine and phosphorus together amounting to at least 2 weight per cent. The initial polyester preferably has an acid value of 70-150, falling after reaction with dicyclodiene to below 70, and to at least 20 less than the original value if this was 70-90. Preferably 0.05-0.6 mols. of dicyclopentadiene are used per mol. of dicarboxylic acid. The dicarboxylic acid (A) is preferably an a ,b -unsaturated dicarboxylic acid, e.g. maleic, fumaric, itaconic, mesaconic, or citraconic acids, or anhydrides or half-esters thereof with a polyhydric alcohol, but may contain preferably not more than 60 equivalent per cent of other acids, e.g. succinic, adipic, sebacic, azelaic, the phthalic and di-, tri-, and tetra-chloro phthalic acids, and tetrahydrophthalic acid, and chlorendic acid. Higher polybasic acids may be used in minor amounts, e.g. pyromellitic or trimellitic acid, the additional carboxy group(s) being esterified with monohydric alcohols. The poly-hydroxy compounds (D) may be, e.g. ethylene glycol, diethylene glycol, 1,2- or 1,3-propanediol, 2,2-dialkanepropadiols, 1,3- and 1,4 - butanediols, D 2.3 - butene - 1,4 - diol, 1,6 - hexanediol, dimethylolbenzenes, resorcinol, the 4,41 - dihydroxy - dicyclohexyl alkanes, the 4,41 - dihydroxy - diphenyl alkanes, trimethylolpropane, glycerol monochlorhydrin, pentaerythritol dichlorohydrin, pentachlorophenyl monoglycerol ether, 4,6-dibromo - resorcinol - bis - (b - hydroxyethyl) ether and 2,3 - bis - [dibromo - 4 - (b - hydroxyethoxy)phenyl] propane. Higher polyhydroxy alcohols may be used, e.g. glycerol, trimethylolpropane or -ethane, the additional hydroxy group(s) being etherified or esterified with monofunctional alcohols or acids. The bromine containing acids (B) are preferably polybasic with at least 2 Br atoms in the molecule, e.g. the bromine additions products of maleic, fumaric, itaconic, mesaconic, and citraconic acids, or of acrylic ricinoleic or linseed oil fatty acids, or di- and tetra-bromophthalic acids, hexabromoendomethylenetetrahydrophthalic acid, dibromohexahydrophthalic acid and dibromoendomethylenehexahydrophthalic acid. The phosphorus compounds (C) may be acids, thio acids, amides, organic oxides, sulphides, esters, thioesters and halides, and include phosphoric acid, phosphorous acid, pyrophosphoric acid, the phosphinic acids and the phosphonic acids and esters and halides thereof, and trimethylol phosphine oxide and tetramethylol phosphonium halides, phosphine sulphides, thiophosphites, thio- and dithio-phosphates, phosphonic amides, amido-phosphites and amido-phosphates. The product resins may be copolymerized with e.g. styrene, alkyland chloro-styrenes, a -methylstyrene, vinyl acetate or propionate, acrylic and methacrylic acid esters, allyl acetate or propionate, diallyl maleate, succinate, adipate, azelate, sebacate, or phthalate, triallyl phosphate, diallyl benzenphosphonate, triallyl cyanurate and N-vinylpyrrolidone. The ratio of vinyl compound to polyester may vary from 4:1 to 1:9, by weight. Conventional polymerization inhibitors, catalysts and accelerators may be used, or an accelerator such as aniline- or p-toluidine-N,N-diacetic acid or N,N-bis-(hydroxyethyl)-aniline or -p-toluidine may be incorporated into the polyester. The product polyesters may also be reacted with polyisocyanates, e.g. 4,41 - diphenylmethane -, 1,5 - naphthalene -, 2,21 - diphenyldimethylmethane - 4,41 -, toluylene-2,4 and toluylene-2,6-, and 1,4-cyclohexylene - diisocyanates, and 4,41,411 - triisocyanatophenyl thiophosphate. Fillers, e.g. asbestos, chalk, powdered glass, silicon carbide, sawdust, hardened plastics, calcium hydrogen phosphate, and glass, cotton, polyester or polyamide fibres, dyes and pigments may be incorporated into moulding compositions. In examples, maleic anhydride is condensed with phthalic anhydride (or bis-hydroxyethyl-terephthalate) and dibromosuccinic or dibromoitaconic acids or tetrabromophthalic anhydride or 9,10,12,13,15,16 - hexabromo - octadecanoic acid, and phosphoric acid or 2-hydroxypropane-2-phosphonic acid or a PCl3/ethylene glycol or vinyl phosphonic dichloride/2,2-dimethylpropanediol-1,3 reaction product, and glycerol, trimethylol propane or 2,2-dimethylpropanediol-1,3 in the presence of hydroquinone and triphenyl phosphite, and the product is reacted with dicyclopentadiene. This product in turn may be copolymerized with styrene (70:30 ratio).
GB44423/64A 1963-10-30 1964-10-30 Improvements in or relating to polyesters Expired GB1031407A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEC0031270 1963-10-30

Publications (1)

Publication Number Publication Date
GB1031407A true GB1031407A (en) 1966-06-02

Family

ID=7019750

Family Applications (1)

Application Number Title Priority Date Filing Date
GB44423/64A Expired GB1031407A (en) 1963-10-30 1964-10-30 Improvements in or relating to polyesters

Country Status (8)

Country Link
US (1) US3333022A (en)
AT (1) AT271013B (en)
BE (1) BE654876A (en)
CH (1) CH496753A (en)
DE (1) DE1495330A1 (en)
GB (1) GB1031407A (en)
NL (1) NL6412649A (en)
SE (1) SE324896B (en)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3619228A (en) * 1966-07-25 1971-11-09 Mac Millan Bloedel Ltd Method of patching wood products using a particular polyester blend
US3536782A (en) * 1967-01-25 1970-10-27 Diamond Shamrock Corp Halogenated polyester compositions and process for preparing the same
US3883612A (en) * 1971-06-07 1975-05-13 Scm Corp Low-shrink thermosetting polymers
US3933757A (en) * 1973-02-08 1976-01-20 Scm Corporation Dicyclopentadiene thermosetting polyester
US3992480A (en) * 1973-07-30 1976-11-16 Hooker Chemicals & Plastics Corporation Fire retardant unsaturated polyesters
JPS5640220A (en) * 1979-09-10 1981-04-16 Hitachi Chem Co Ltd Manufacturing of flyback transformer
US4525427A (en) * 1982-09-20 1985-06-25 The Alpha Corporation Polyester primer composition and method
US5043374A (en) * 1988-03-25 1991-08-27 Atochem North America, Inc. Halogenated polyester flame retardants for polyphenylene ether, polyolefin and polyethylene terephthalate resins
CN102227480B (en) 2008-11-26 2014-09-03 威士伯采购公司 Polyester-carbamate polymer and coating compositions thereof
EP2370490B1 (en) 2008-11-26 2018-07-18 Valspar Sourcing, Inc. Coating compositions comprising a polyester polymer
US20100260954A1 (en) * 2008-11-26 2010-10-14 Valspar Sourcing, Inc. Polymer having polycyclic groups and coating compositions thereof
US8367171B2 (en) 2008-11-26 2013-02-05 Valspar Sourcing, Inc. Polymer having polycyclic groups and coating compositions thereof
ES2595990T3 (en) 2009-04-09 2017-01-04 Valspar Sourcing, Inc. Polymer having unsaturated cycloaliphatic functionality and coating compositions formed therefrom
CN102388080B (en) 2009-04-09 2014-09-24 威士伯采购公司 Polyester coating composition

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL274611A (en) * 1951-01-28
US2671070A (en) * 1951-12-08 1954-03-02 Us Rubber Co Reaction products of dicyclopentadiene, maleic anhydride, and a glycol, and copolymers thereof
US2819247A (en) * 1953-06-10 1958-01-07 American Cyanamid Co Flame-resistant polyester resinous compositions containing combined halogens and phosporus and process of preparation
DE1178211B (en) * 1955-01-29 1964-09-17 C F Roser G M B H Process for the production of unsaturated polyester
US2852487A (en) * 1955-08-05 1958-09-16 Glidden Co Polymerizable solution of an allyl ether and an unsaturated alkyd resin
US2951823A (en) * 1956-02-11 1960-09-06 Ruetgerswerke Ag Unsaturated polyesters of unsaturated alpha, beta-dicarboxylic acids and polyvalent alcohols
DE1150203B (en) * 1959-08-25 1963-06-12 Distillers Co Yeast Ltd Process for the production of an unsaturated polyester
FR1317444A (en) * 1962-02-12 1963-02-08 Albert Ag Chem Werke Process for preparing polyester resins

Also Published As

Publication number Publication date
NL6412649A (en) 1965-05-03
CH496753A (en) 1970-09-30
BE654876A (en) 1965-04-27
US3333022A (en) 1967-07-25
DE1495330A1 (en) 1969-02-27
SE324896B (en) 1970-06-15
AT271013B (en) 1969-05-27

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